Listerine FreshBurst Antiseptic description, usages, side effects, indications, overdosage, supplying and lots more!

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Listerine FreshBurst Antiseptic

Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Listerine FreshBurst Antiseptic


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purposes
Eucalyptol 0.092% }
Menthol 0.042% }
Methyl salicylate 0.060% }
Thymol 0.064% }
Antiplaque/antigingivitis

Listerine FreshBurst Antiseptic Uses

helps prevent and reduce:

  • plaque
  • gingivitis

Warnings

Do not use in children under 12 years of age

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • rinse full strength for 30 seconds with 20 ml (2/3 fluid ounce or 4 teaspoonfuls) morning and night
  • do not swallow

Listerine FreshBurst Antiseptic Other information

  • store at room temperature
  • cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

water, alcohol (21.6%), sorbitol solution, flavoring, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, D&C yellow no. 10, FD&C green no. 3

Questions?

call 1-888-222-0182, weekdays

Dist: Johnson & Johnson Healthcare Products
Division of McNEIL-PPC, Inc.
Skillman, NJ 08558-9418 USA

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

LISTERINE®
FRESHBURST®
ANTISEPTIC

Kills Germs that Cause
Bad Breath, Plaque & the
Gum Disease Gingivitis

ADA
Accepted
American
Dental Association®

500 mL (1.05 Pt)

Listerine FreshBurst Antiseptic

Listerine FreshBurst Antiseptic

Eucalyptol, Menthol, Methyl Salicylate, and Thymol MOUTHWASH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-403
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EUCALYPTOL EUCALYPTOL 0.92 mg
MENTHOL 0.42 mg
methyl salicylate METHYL SALICYLATE 0.6 mg
THYMOL THYMOL 0.64 mg

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
sorbitol
POLOXAMER 407
BENZOIC ACID
SACCHARIN SODIUM DIHYDRATE
SODIUM BENZOATE
D&C YELLOW NO. 10
FD&C GREEN NO. 3

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42002-403-73 250 in 1 BOTTLE, PLASTIC
2 NDC:42002-403-72 500 in 1 BOTTLE, PLASTIC
3 NDC:42002-403-71 1000 in 1 BOTTLE, PLASTIC
4 NDC:42002-403-70 1500 in 1 BOTTLE, PLASTIC
5 NDC:42002-403-63 3700 in 1 BOTTLE, PLASTIC
6 NDC:42002-403-70 1500 in 1 BOTTLE, PLASTIC
7 NDC:42002-403-94 2 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2012-02-21


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